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01 3ALLERGAN

02 3ACCORD HLTHCARE

03 1ACTAVIS ELIZABETH

04 18ACTAVIS LABS FL INC

05 12ALEMBIC

06 6AMTA

07 12APOTEX

08 4APOTHECON

09 21BAUSCH

10 14BIOVAIL

11 2BIOVAIL LABS INTL

12 4CHARTWELL MOLECULES

13 6CHARTWELL RX

14 1DR REDDYS

15 3DR REDDYS LABS SA

16 4EDENBRIDGE PHARMS

17 1EUGIA PHARMA

18 2EXELA PHARMA

19 3GLENMARK PHARMS LTD

20 1HIKMA

21 3HIKMA FARMACEUTICA

22 4HOSPIRA

23 2HQ SPCLT PHARMA

24 1INTL MEDICATION

25 4IVAX SUB TEVA PHARMS

26 5MACLEODS PHARMS LTD

27 3MYLAN

28 1MYLAN LABS LTD

29 6NESHER PHARMS

30 8NOVAST LABS

31 5PH HEALTH

32 3PHARMOBEDIENT

33 5RISING

34 1SAGENT

35 10SCIEGEN PHARMS

36 15SUN PHARM

37 9TEVA

38 4TEVA PHARMS

39 8TWI PHARMS

40 6UTOPIC PHARMS

41 4VALEANT PHARMS NORTH

42 4ZYDUS LIFESCIENCES

43 11ZYDUS PHARMS

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PharmaCompass

01

DILTIAZEM HYDROCHLORIDE

Brand Name : DILACOR XR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-05-29

Application Number : 20092

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie CB

02

DILTIAZEM HYDROCHLORIDE

Brand Name : DILACOR XR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-05-29

Application Number : 20092

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie CB

03

DILTIAZEM HYDROCHLORIDE

Brand Name : DILACOR XR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-05-29

Application Number : 20092

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie CB

04

PEGS Boston Summit
Not Confirmed
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PEGS Boston Summit
Not Confirmed

DILTIAZEM HYDROCHLORIDE

Brand Name : CARDIZEM

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Approval Date : 1982-11-05

Application Number : 18602

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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05

PEGS Boston Summit
Not Confirmed
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PEGS Boston Summit
Not Confirmed

DILTIAZEM HYDROCHLORIDE

Brand Name : CARDIZEM

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG

Approval Date : 1982-11-05

Application Number : 18602

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

06

PEGS Boston Summit
Not Confirmed
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PEGS Boston Summit
Not Confirmed

DILTIAZEM HYDROCHLORIDE

Brand Name : CARDIZEM

Dosage Form : TABLET;ORAL

Dosage Strength : 90MG

Approval Date : 1986-12-08

Application Number : 18602

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

07

PEGS Boston Summit
Not Confirmed
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PEGS Boston Summit
Not Confirmed

DILTIAZEM HYDROCHLORIDE

Brand Name : CARDIZEM

Dosage Form : TABLET;ORAL

Dosage Strength : 120MG

Approval Date : 1986-12-08

Application Number : 18602

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

08

PEGS Boston Summit
Not Confirmed
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PEGS Boston Summit
Not Confirmed

DILTIAZEM HYDROCHLORIDE

Brand Name : CARDIZEM SR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1989-01-23

Application Number : 19471

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

09

PEGS Boston Summit
Not Confirmed
arrow
arrow
PEGS Boston Summit
Not Confirmed

DILTIAZEM HYDROCHLORIDE

Brand Name : CARDIZEM SR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1989-01-23

Application Number : 19471

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

PEGS Boston Summit
Not Confirmed
arrow
arrow
PEGS Boston Summit
Not Confirmed

DILTIAZEM HYDROCHLORIDE

Brand Name : CARDIZEM SR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1989-01-23

Application Number : 19471

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank